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Mbio|November 11, 2024
Microbiome-producing SCFAs are associated with preterm birth via trophoblast function modulationLulu Meng, Meng Meng, Ruonan Zhang, et al.
Acta Obstetricia Et Gynecologica Scandinavica|June 27, 2023
Optical genome mapping for detection of chromosomal aberrations in prenatal diagnosisQinxin Zhang, Yan Wang, Yiyun Xu, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|December 29, 2023
Residual risk of clinically significant copy number variations in fetuses with nasal bone absence or hypoplasia after excluding non-invasive prenatal screening-detectable findingsZhengyi Xia, Ran Zhou, Yiyun Xu, et al.
Archives of Gynecology and Obstetrics|June 8, 2026
NIPT-based prenatal screening of maternal Xq28 copy number variations in a cohort of 80,371 pregnanciesLulu Meng, Yiyun Xu, Yixuan Liang, et al.
Taiwanese Journal of Obstetrics & Gynecology|October 18, 2017
Noninvasive prenatal diagnosis for X-linked disease by maternal plasma sequencing in a family of Hemophilia BPing Hu, Fengchang Qiao, Yuan Yuan, et al.
Frontiers in Cardiovascular Medicine|June 24, 2021
Analysis of Biomarkers for Congenital Heart Disease Based on Maternal Amniotic Fluid MetabolomicsYahong Li, Yun Sun, Lan Yang, et al.
American Journal of Obstetrics and Gynecology|November 13, 2017
Prenatal chromosomal microarray analysis in fetuses with congenital heart disease: a prospective cohort studyYan Wang, Li Cao, Dong Liang, et al.
American Journal of Medical Genetics. Part A|March 27, 2015
FLCN intragenic deletions in Chinese familial primary spontaneous pneumothoraxYibing Ding, Chengchu Zhu, Wei Zou, et al.
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